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Strategic redox relay enables a scalable synthesis of ouabagenin, a bioactive cardenolide.


ABSTRACT: Here, we report on a scalable route to the polyhydroxylated steroid ouabagenin with an unusual take on the age-old practice of steroid semisynthesis. The incorporation of both redox and stereochemical relays during the design of this synthesis resulted in efficient access to more than 500 milligrams of a key precursor toward ouabagenin-and ultimately ouabagenin itself-and the discovery of innovative methods for carbon-hydrogen (C-H) and carbon-carbon activation and carbon-oxygen bond homolysis. Given the medicinal relevance of the cardenolides in the treatment of congestive heart failure, a variety of ouabagenin analogs could potentially be generated from the key intermediate as a means of addressing the narrow therapeutic index of these molecules. This synthesis also showcases an approach to bypass the historically challenging problem of selective C-H oxidation of saturated carbon centers in a controlled fashion.

SUBMITTER: Renata H 

PROVIDER: S-EPMC4365795 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Strategic redox relay enables a scalable synthesis of ouabagenin, a bioactive cardenolide.

Renata Hans H   Zhou Qianghui Q   Baran Phil S PS  

Science (New York, N.Y.) 20130101 6115


Here, we report on a scalable route to the polyhydroxylated steroid ouabagenin with an unusual take on the age-old practice of steroid semisynthesis. The incorporation of both redox and stereochemical relays during the design of this synthesis resulted in efficient access to more than 500 milligrams of a key precursor toward ouabagenin-and ultimately ouabagenin itself-and the discovery of innovative methods for carbon-hydrogen (C-H) and carbon-carbon activation and carbon-oxygen bond homolysis.  ...[more]

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